Canonical Allele Identifier: CA382436082

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922171C>G (hg19) ; chr11:g.101051440C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051440C>G , CM000673.2:g.101051440C>G	GRCh38
NC_000011.9:g.100922171C>G , CM000673.1:g.100922171C>G	GRCh37
NC_000011.8:g.100427381C>G	NCBI36
NG_016475.1:g.83374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2341G>C MANE Select	ENSP00000325120.5:p.Asp781His
ENST00000263463.9:c.2035G>C	ENSP00000263463.5:p.Asp679His
ENST00000325455.9:c.2341G>C	ENSP00000325120.5:p.Asp781His
ENST00000526300.5:c.2035G>C	ENSP00000436803.1:p.Asp679His
ENST00000528960.5:c.2224G>C	ENSP00000432914.1:p.Asp742His
ENST00000530764.1:n.31G>C
ENST00000533207.5:n.1708G>C
ENST00000534013.5:c.559G>C	ENSP00000436561.1:p.Asp187His
ENST00000534780.5:c.2341G>C	ENSP00000432352.1:p.Asp781His
ENST00000617858.4:c.2035G>C	ENSP00000481227.1:p.Asp679His
ENST00000619228.2:c.2224G>C	ENSP00000482698.1:p.Asp742His
NM_000926.4:c.2341G>C MANE Select	NP_000917.3:p.Asp781His
NM_001202474.3:c.1849G>C	NP_001189403.1:p.Asp617His
NM_001271161.2:c.1543G>C	NP_001258090.1:p.Asp515His
NM_001271162.1:c.559G>C	NP_001258091.1:p.Asp187His
NR_073141.2:n.2334G>C
NR_073142.2:n.2217G>C
NR_073143.2:n.2028G>C
XM_006718858.2:c.2341G>C	XP_006718921.1:p.Asp781His
XM_006718858.3:c.2341G>C	XP_006718921.1:p.Asp781His
NM_001271162.2:c.559G>C	NP_001258091.1:p.Asp187His
NR_073141.3:n.2348G>C
NR_073142.3:n.2231G>C
NR_073143.3:n.2042G>C